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Infantile Encephaloneuromyopathy and Defective Mitochondrial Translation Are Due to a Homozygous RMND1 Mutation

✍ Scribed by Beatriz Garcia-Diaz; Mario H. Barros; Simone Sanna-Cherchi; Valentina Emmanuele; Hasan O. Akman; Claudia C. Ferreiro-Barros; Rita Horvath; Saba Tadesse; Nader El Gharaby; Salvatore DiMauro; Darryl C. De Vivo; Aly Shokr; Michio Hirano; Catarina M. Quinzii

Book ID: 119184381
Publisher: American Society of Human Genetics
Year: 2012
Tongue: English
Weight: 722 KB
Volume: 91
Category: Article
ISSN: 0002-9297
DOI: 10.1016/j.ajhg.2012.08.019

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